Auberger's blood group

From WikiMD's Food, Medicine & Wellness Encyclopedia

Auberger's blood group system is a classification of human blood based on the presence or absence of specific antigens on the surface of red blood cells. It is one of the many blood group systems recognized by immunohematologists, contributing to the complexity of human blood typing beyond the well-known ABO and Rh systems. The Auberger blood group system is of particular interest in the fields of transfusion medicine and immunogenetics due to its implications in blood transfusion reactions and maternal-fetal incompatibility.

Overview[edit | edit source]

The Auberger blood group system is identified by the presence of specific antigens, designated as Aub antigens, on the surface of red blood cells. These antigens are proteins or glycoproteins that can elicit an immune response if they are foreign to the body. The system is genetically determined, with the antigens being inherited from one's parents. The presence or absence of Aub antigens defines the Auberger blood group of an individual.

Genetics[edit | edit source]

The genetic basis of the Auberger blood group system involves a gene or genes that encode for the synthesis of the Aub antigens. The exact genetic loci and the molecular mechanisms involved in the expression of Aub antigens are subjects of ongoing research. However, it is known that the inheritance pattern follows Mendelian principles, with alleles determining the presence or absence of the antigens.

Clinical Significance[edit | edit source]

The clinical significance of the Auberger blood group system lies in its potential to cause transfusion reactions and hemolytic disease of the newborn (HDN). In transfusion medicine, the compatibility of Auberger antigens between donor and recipient is crucial to prevent adverse reactions. Although reactions related to this system are rare, they can occur if blood transfusion is performed without proper matching.

In the context of pregnancy, the Auberger system can contribute to HDN, a condition where the mother's immune system attacks the fetal red blood cells. This occurs if the mother lacks Aub antigens and the fetus inherits them from the father, leading to the production of maternal antibodies against the fetal cells.

Diagnosis and Testing[edit | edit source]

Diagnosis of the Auberger blood group involves serological testing to detect the presence or absence of Aub antigens on the red blood cells. This is typically done using specific antisera in a laboratory setting. Genetic testing may also be employed to identify alleles associated with the Auberger system.

Management[edit | edit source]

Management of issues related to the Auberger blood group system involves careful blood typing and cross-matching in transfusion scenarios to ensure compatibility. In cases of HDN, treatment may include intrauterine transfusions or exchange transfusions after birth, depending on the severity of the condition.

Conclusion[edit | edit source]

The Auberger blood group system, while less commonly encountered than the ABO or Rh systems, plays a significant role in transfusion medicine and immunogenetics. Understanding and recognizing the importance of this system can aid in preventing transfusion-related complications and managing HDN effectively.

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